Roxarsone transformation and its impacts on soil enzyme activity in paddy soils: A new insight into water flooding effects.

The aromatic arsenical roxarsone (ROX) has been used as feed additive for decades worldwide. The past or present application of animal manure containing ROX in paddy fields results in arsenic (As) accumulation in rice grain. However, the degradation and transformation mechanisms of ROX in paddy soil which determine As bioavailability and uptake by rice are still unclear. The current study investigated the variation of As speciation and soil enzyme activities in ROX-treated soils under flooded and non-flooded conditions for six months. Our results showed that 70.2% of ROX persisted in non-flooded paddy soils after 180 d while ROX degraded completely within 7 d in flooded soils. The rapid degradation of ROX under flooded conditions owed to the enhanced biotic transformation that was caused by the low Eh and the predominant presence of Clostridium spp. and Bacillus spp. ROX was not only transformed to As(III) and As(V) in non-flooded soils but also to 3-amino-4-hydroxyphenylarsonic acid and methyl arsenicals in flooded soils. The degradation products significantly inhibited soil enzyme activities for 7-30 d, but the inhibition effects disappeared after 90 d due to the sorption of transformed As products to amorphous Fe oxides. This study provides new insights into the flooding effect on ROX fate in paddy fields, which is important for the management of animal waste and risk control on polluted sites.

Improvement of water quality in the Pearl River Estuary, China: a long-term (2008-2017) case study of temporal-spatial variation, source identification and ecological risk of heavy metals in surface water of Guangzhou.

A series of environmental protective policies have been taken recently in the Pearl River Estuary (PRE) to alleviate water pollution; however, their influence on the reduction of heavy metals in estuarine water has not been known. This study selected Guangzhou as a representative city in the PRE and collected estuarine water monthly from 2008 to 2017 to track the variation of As, Hg, Pb, Cd, Cu, Zn, and Se. During the last decade, the high time-resolved record showed that the concentration of Hg, Pb, Cd, Cu, and Zn in estuarine water reduced by 39.5%, 91.0%, 86.2%, 74.6%, and 97.3%, respectively. However, the concentration of As kept in a stable range (1.89-2.69 µg L-1) and Se (0.17-0.65 µg L-1) increased slightly. The principal component analysis (PCA) and absolute principal component scores-multiple linear regression (APCS-MLR) results suggested that the upstream industrial effluents were major sources for Hg (45.5-92.7%), Pb (47.3-100%), Cd (42.0-90.6%), Cu (85.5-100%), and Zn (100%) and the geogenic source was major origin for As (84.6-98.3%) and Se (0-67.5%). The risk quotient of Hg, Pb, Cd, Cu, and Zn to aquatic organisms largely decreased from 0.03, 0.59, 0.03, 2.06, and 0.26 in 2008 to 0.02, 0.05, 0.006, 0.52, and 0.007 in 2017, respectively. The effective control of heavy metal pollution in the study area can be primarily due to the relocation of hundreds of polluting factories during the last decade.